FDA Adverse Event Injury Summary report: N

RESTORE 5X10 SELF-TAPPING IMPLANT WITH MOUNT

MDR report key: 188219 · Received September 21, 1998

Report

Report Number
2184002-1998-00666
Event Type
Injury
Date Received
September 21, 1998
Date of Event
August 19, 1998
Report Date
September 21, 1998
Manufacturer
LIFECORE BIOMEDICAL, INC.
Product Code
DZE
Removal / Correction Number
NA
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
MI, US
Reporter Occupation
DENTIST

Narratives

Description of Event or Problem · 1

IMPLANT PLACED 01/15/1998. IT FAILED DUE TO MOBILITY AND WAS REMOVED 08/19/1998.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
1 RESTORE 5X10 SELF-TAPPING IMPLANT WITH MOUNT Implant ENDOSSEOUS IMPLANT DZE LIFECORE BIOMEDICAL, INC. R9010-50-10 75970591

Patients

Seq Age Sex Outcome Treatment
1 59 YR Required Intervention